Quaternised renzapride as a potent and selective 5-HT4 receptor agonist-Reference-Cited by-同舟云学术

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Quaternised renzapride as a potent and selective 5-HT4 receptor agonist

Published:1993-04 Issue:4 Volume:3 Page:633-634
ISSN:0960-894X
Container-title:Bioorganic & Medicinal Chemistry Letters
language:en
Short-container-title:Bioorganic & Medicinal Chemistry Letters

Author:

Baxter G.S.,Boyland P.,Gaster L.M.,King F.D.

Publisher

Elsevier BV

Subject

Organic Chemistry,Clinical Biochemistry,Drug Discovery,Pharmaceutical Science,Molecular Biology,Molecular Medicine,Biochemistry

Reference16 articles.

1. The gastrointestinal prokinetic benzamide derivatives are agonists at the non-classical 5-HT receptor (5-HT4) positively coupled to adenylate cyclase in neurons

2. 5-Hydroxytryptamine4 receptors mediate relaxation of the rat oesophageal tunica muscularis mucosae

Cited by 14 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. 5-HT4 Receptors;Current Drug Target -CNS & Neurological Disorders;2004-02-01

2. 5-HT4 Receptors: An Update;Serotoninergic Neurons and 5-HT Receptors in the CNS;2000

3. 2,3-Dihydro-2-oxo-1H-benzimidazole-1-carboxamides with Selective Affinity for the 5-HT4 Receptor: Synthesis and Structure−Affinity and Structure−Activity Relationships of a New Series of Partial Agonist and Antagonist Derivatives;Journal of Medicinal Chemistry;1999-07-01

4. Medicinal Chemistry of 5-HT4 Receptor Ligands;5-HT4 Receptors in the Brain and Periphery;1998

5. The Effects of Novel, Selective 5-Hydroxytryptamine (5-HT) 4 Receptor Ligands in Rat Spatial Navigation;Neuropharmacology;1997-04

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